Schmiedeberg Lars, Skene Pete, Deaton Aimée, Bird Adrian
Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
PLoS One. 2009;4(2):e4636. doi: 10.1371/journal.pone.0004636. Epub 2009 Feb 27.
Formaldehyde crosslinking is in widespread use as a biological fixative for microscopy and molecular biology. An assumption behind its use is that most biologically meaningful interactions are preserved by crosslinking, but the minimum length of time required for an interaction to become fixed has not been determined.
Using a unique series of mutations in the DNA binding protein MeCP2, we show that in vivo interactions lasting less than 5 seconds are invisible in the microscope after formaldehyde fixation, though they are obvious in live cells. The stark contrast between live cell and fixed cell images illustrates hitherto unsuspected limitations to the fixation process. We show that chromatin immunoprecipitation, a technique in widespread use that depends on formaldehyde crosslinking, also fails to capture these transient interactions.
CONCLUSIONS/SIGNIFICANCE: Our findings for the first time establish a minimum temporal limitation to crosslink chemistry that has implications for many fields of research.
甲醛交联作为一种用于显微镜检查和分子生物学的生物固定剂被广泛使用。其使用背后的一个假设是,大多数具有生物学意义的相互作用通过交联得以保留,但相互作用变得固定所需的最短时间尚未确定。
通过在DNA结合蛋白MeCP2中使用一系列独特的突变,我们发现,甲醛固定后,持续时间少于5秒的体内相互作用在显微镜下不可见,尽管它们在活细胞中很明显。活细胞图像与固定细胞图像之间的鲜明对比说明了固定过程中迄今未被怀疑的局限性。我们表明,广泛使用的依赖甲醛交联的染色质免疫沉淀技术也无法捕捉到这些瞬时相互作用。
结论/意义:我们的研究结果首次确定了交联化学的最小时间限制,这对许多研究领域都有影响。